Validation Specialist

Kelly Engineering has an exciting Validation Specialist project (10 months) with an industry leader onsite in Parsippany, NJ. This role offers a competitive pay rate based on experience and the opportunity to work with an impactful product in a positive team environment.**PLEASE NOTE WE ARE NOT ABLE TO DO C2C FOR THIS ROLE**Validation Specialist Responsibilities:Validation documentation for manufacturing (PLC, HMI, SCADA) and quality systems, ensuring efficiency, reliability, and compliance with industry standardsDesign and develop validation documents, system manuals, configuration specifications, user requirement specifications, summary reports, risk assessment documents.Document all validation activities, including test results, deviations, and corrective actionsPrepare comprehensive validation reports and maintain accurate records in accordance with company policies and regulatory guidelinesWork closely with engineering, quality assurance, and production teamsValidation Specialist RequirementsKnowledge of FDA's 21 CFR Part 11 requiredExperience writing Validation documentation for manufacturing and quality systems- PLC, HMI, SCADA a plusExcellent analytical, problem-solving abilities, and attention to detail.What happens next:Once you apply, you'll proceed to next steps if your skills and experience look like a good fit. But don't worry - even if this position doesn't work out, you're still in the Kelly Engineering network. That means our team of expert engineering recruiters will have access to your profile, making your opportunities limitless.

Created: 2025-02-23